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rs281860418

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860418(A;C)
Make rs281860418(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271632
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860418
ebirs281860418
HLIrs281860418
Exacrs281860418
Varsomers281860418
Maprs281860418
PheGenIrs281860418
hapmaprs281860418
1000 genomesrs281860418
hgdprs281860418
ensemblrs281860418
gopubmedrs281860418
geneviewrs281860418
scholarrs281860418
googlers281860418
pharmgkbrs281860418
gwascentralrs281860418
openSNPrs281860418
23andMers281860418
23andMe allrs281860418
SNP Nexus

SNPshotrs281860418
SNPdbers281860418
MSV3drs281860418
GWAS Ctlgrs281860418
Max Magnitude0
ClinVar
Risk rs281860418(C,G;C,G)
Alt rs281860418(C,G;C,G)
Reference rs281860418(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239409T>C; NC_000006.11:g.31239409T>G
CLNSRC
CLNACC